Cas 1111649-94-5,ethyl (2ξ,4E)-5-{2-[(3ξ)-5-methoxy-3-methyl-5-oxopent-3-en-1-yl]phenyl}-3-methylpenta-2,4-dienoate

1111649-94-5

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Basic information

Product Name: ethyl (2ξ,4E)-5-{2-[(3ξ)-5-methoxy-3-methyl-5-oxopent-3-en-1-yl]phenyl}-3-methylpenta-2,4-dienoate
Synonyms:
CAS NO:1111649-94-5
Molecular Formula:
Molecular Weight: 342.435
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl (2ξ,4E)-5-{2-[(3ξ)-5-methoxy-3-methyl-5-oxopent-3-en-1-yl]phenyl}-3-methylpenta-2,4-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2ξ,4E)-5-{2-[(3ξ)-5-methoxy-3-methyl-5-oxopent-3-en-1-yl]phenyl}-3-methylpenta-2,4-dienoate(1111649-94-5)
EPA Substance Registry System: ethyl (2ξ,4E)-5-{2-[(3ξ)-5-methoxy-3-methyl-5-oxopent-3-en-1-yl]phenyl}-3-methylpenta-2,4-dienoate(1111649-94-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1111649-94-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1111649-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,6,4 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1111649-94:
(9*1)+(8*1)+(7*1)+(6*1)+(5*6)+(4*4)+(3*9)+(2*9)+(1*4)=125
125 % 10 = 5
So 1111649-94-5 is a valid CAS Registry Number.

1111649-94-5Upstream product

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1111649-94-5Relevant academic research and scientific papers

Synthesis of aryl-containing terpenoids based on 1,4-dihydronaphthalene

Kukovinets,Kislitsyn,Zainullin,Mukhamedzyanova,Galin,Abdullin

, p. 362 - 368 (2008)

Successive transformations including oxidation of 1,4-dihydronaphthalene into 1,2,3,4-tetrahydronaphthalen-2-one, Reformatskii reaction of the latter with methyl bromoacetate, ozonolysis of the Reformatsky reaction product, and Emmons olefination of the aldehyde group in methyl 3-oxo-5-(2-formylphenyl) pentanate thus formed gave analogs of highly active dienoate juvenoids having an aromatic ring in their molecules.

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